rs1555734932

This variant is located in the LGI4 gene.

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ClinVar annotation

Likely Pathogenic

1 submitter

Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect

About LGI4

Involved in regulation of myelination. Predicted to be located in extracellular region. Predicted to be active in extracellular space. Implicated in arthrogryposis multiplex congenita-1 and childhood absence epilepsy. [provided by Alliance of Genome Resources, Jul 2025]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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